Clinical Investigation to Assess the Safety and Feasibility of the Crestal, Minimal-invasive Sinus Floor Augmentation With the Pressure Chamber Drill (DKK) and the Sinus Vibration Pump (SVP)

NCT ID: NCT01204424

Last Updated: 2010-09-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE1

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-09-30

Study Completion Date

2011-06-30

Brief Summary

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The success of dental implants is based on a variety of factors including; surgical technique, health of the patient, operator skill and, to a significant part, sufficient bone for the placement and integration of dental implants. To that end, the replacement of the maxillary posterior teeth have presented a considerable challenge because, after the loss of maxillary posterior teeth the quality and quantity of the remaining supporting bone may be insufficient to support implants properly or reliably. To overcome the deficiency of insufficient vertical bone mass of the maxilla, several surgical techniques have been developed to increase available bone mass for the replacement of dental implants by bone augmentation.

The conventional procedure for a sinus lift (Caldwell-Luc procedure) requires preparation of a mucoperiosteal flap in the buccal molar region and to cut an oval window in the thus exposed bone, without damage to the subjacent maxillary sinus membrane. The procedure is very invasive and subjects the patient to great stress as a result of substantial swelling and discoloration of up to 10 days, and possibly of pain. This surgical procedure is oftentimes referred to as "open" or "classic" sinus lift. This technique is fraught with many risks and complications because of the limitations of healing potential in the maxillary sinus. In spite of these risks many patients undergo this procedure because of the strong desire to replace missing maxillary teeth with dental implants.

An alternative approach to the maxillary sinus from the inferior approach of the alveolar ridge utilizing solid cylindrical osteotomes was described by Dr. Summers (crestal sinus lift). It is a more conservative approach and is less invasive. It was developed to eliminate the risks described above.While this technique is safer, an overzealous use of an osteotome during the placement of the regenerative material can result in the perforation of the subantral membrane with disadvantages discussed above.

Dr. Eder has developed an innovative way - the JEDER System - of carrying out a crestal sinus lift that substantially reduces the risk of perforating the subantral membrane. This minimal- invasive way uses 2 newly developed and successfully patented instruments, the "Druckkammerknochenfräse" DKK and the "Sinusvibrationspumpe" SVP. Following JEDER Syst. the mucous membrane of the mouth is opened from the toothless part of the maxillary crest up to the bone and the bone is scraped by a cylindrical cutter in the shape of a tunnel up to slightly underneath the maxillary sinus membrane.

The aim of the study is to assess the efficacy and safety of the JEDER Syst., which was already demonstrated in 50 treatment attempts. The results of this study will be used for the certification process to enable the declaration of conformity for the market approval.

The main outcome parameter is the perforation rate of the subantral membrane intraoperatively and within 6 weeks after the operation.

Risk benefit assessment:

In the present study there will be no additional examinations undertaken compared to patients which undergo the conventional procedure. The conventional procedure is associated with a risk of membrane perforation and consecutive diseases like infection, swelling and pain. All these inconveniences should be avoided by using the JEDER Syst. If the worst case scenario - the perforation of the subantral membrane - happens, the conventional method will be used. Therefore, the risk-benefit assessment

Detailed Description

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Conditions

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Insufficient Bone Mass in the Maxilla for Dental Implants

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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minimal-invasive sinus floor augmentation with the DKK and SVP (JEDER Syst.)

minimal-invasive sinus floor augmentation with the DKK and SVP (JEDER Syst.)

Intervention Type DEVICE

minimal invasive crestal sinus lift with the JEDER Systh.

The mucous membrane is opened from the toothless part of the maxillary crest up to the bone and the bone is scraped by a cylindrical cutter in the shape of a tunnel up to slightly underneath the maxillary sinus membrane and hydraulic pressure is being built up within the DKK. A centrally placed drill within the DKK slowly moves in the direction of the membrane. At the moment of the first minimal perforation of the remaining bone the pressurized fluid pushes the membrane back and ensures that the membrane is not perforated by the drill.

The SVP is used to generate hydraulic vibrations, which help to further raise the membrane from the bone (principle of the "percussion drill"). After the maxillary sinus membrane has successfully been elevated, the working fluid is extracted and bone replacement material is introduced via the bore.

Intervention Type DEVICE

Other Intervention Names

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minimal invasive crestal sinuslift

Eligibility Criteria

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Inclusion Criteria

* demand for sinus floor elevation (regio 4 to 7)
* loss of teeth (regio 4 to 7)
* needed extraction of teeth (regio 4 to 7)

Exclusion Criteria

* maxillary bone mass \<3mm
* severe chronic illness or immune deficiency
* cortisone therapy
* sinus membrane membrane hight \>5mm
* chronic sinusitis
* smoking \>20 Zigarettes
* missing dental hygiene
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Jeder GmbH

INDUSTRY

Sponsor Role lead

Responsible Party

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JEDER GmbH

Principal Investigators

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Michaela M Bayerle-Eder, Prof., MD, MBA

Role: STUDY_DIRECTOR

Medical University Vienna, Vienna Austria, Europe

Locations

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Ordination Dr. Klaus Eder

Vienna, Vienna, Austria

Site Status RECRUITING

Countries

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Austria

Central Contacts

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Andreas Bayerle, MBA

Role: CONTACT

Michaela Bayerle-Eder, Prof.,

Role: CONTACT

Other Identifiers

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EK_10_101_0610

Identifier Type: OTHER

Identifier Source: secondary_id

DKK-SVP-10 Prot. 1.4

Identifier Type: -

Identifier Source: org_study_id